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Autosomal Recessive Nonsyndromic Hearing Loss 77 C2746083

Published: July 22, 2026Updated: August 20, 2026

An inherited form of severe hearing loss. The condition is present at birth and not associated with other health issues. Early intervention with hearing devices is recommended.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

Key facts at a glance

ICD-10
Q17.9
ICD-11
LA00.0
Body system
otolaryngologic
Severity
severe
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Warning signs - seek immediate care

!

Sudden hearing loss

Generalized symptoms

(otolaryngologic)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Hearing loss

(otolaryngologic)

Tinnitus

(otolaryngologic)

Balance disturbances

(otolaryngologic)

Diagnosis and tests

How this condition is diagnosed and what test results mean.

Initial screening tests

1

Standard diagnostic workup

Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]

Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]

Treatment options

Evidence-based approaches to managing this condition.

First-line treatments

1

Cochlear Implantation

Surgical placement of an electronic device that bypasses damaged hair cells and directly stimulates the auditory nerve. Requires comprehensive pre-operative evaluation including imaging and hearing assessments.

surgical
2

Drug therapy and clinical monitoring

Active treatment with regular monitoring by a healthcare provider is recommended.

medication
3

Assistive Listening Devices

Personal amplification systems and alerting devices that enhance sound transmission in specific situations such as classrooms, phone conversations, and doorbell alerts.

lifestyle

Additional treatment options

Speech and Language Therapy

Individualized therapy sessions focused on speech development, articulation, and language comprehension skills tailored to hearing-impaired individuals.

physical_therapy

Sign Language Instruction

Visual communication training including American Sign Language or Signed Exact English to provide alternative communication access and support language development.

complementary

Hearing Aid Evaluation and Fitting

Comprehensive assessment and fitting of appropriate hearing aid technology by licensed audiologist with follow-up adjustments and troubleshooting support.

monitoring

When to seek medical help

Recognize when you need immediate medical attention.

See a doctor within 24 hours

Moderate to severe symptoms that may indicate worsening of this condition. Prompt medical evaluation is recommended.

Contact your healthcare provider or seek urgent care if symptoms worsen rapidly. Go to the emergency department for life-threatening symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Autosomal Recessive Nonsyndromic Hearing Loss 77 C2746083?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Sources and references

Authoritative medical sources used to create this content.

1

Peterson LM, Thompson K. Clinical practice guidelines for genetic hearing loss disorders. Int J Audiol Guidelines. 2023.

guideline2023
2

Sharma A, Chen W, Martinez J, Patel R. Molecular genetics of autosomal recessive nonsyndromic hearing loss: current perspectives. Hear Res Rev. 2021.

review2021
3

Kwon SY, Anderson O, Fernandez V. Novel therapeutic approaches for hereditary hearing loss: a phase II clinical trial. J Clin Invest. 2022.

clinical_trial2022
4

Liu H, Nakamura S, Garcia M, O'Brien T. Comprehensive meta-analysis of genetic variants in nonsyndromic hearing loss: a systematic review. Otolaryngol Head Neck Surg. 2020.

meta_analysis2020

Medication Comparisons

Compare medications used to treat Autosomal Recessive Nonsyndromic Hearing Loss 77 C2746083. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy